Battery

ABSTRACT

A battery capable of improving the energy density and improving the battery characteristics such as cycle characteristics and high temperature storage characteristics is provided. A cathode and an anode are oppositely arranged with a separator in between. The open circuit voltage in full charge is in the range from 4.25 V to 6.00 V. The separator has a base material layer and a surface layer. The surface layer opposed to the cathode is formed from at least one from the group consisting of polyvinylidene fluoride, polytetrafluoroethylene, polypropylene, and aramid.

CROSS REFERENCES TO RELATED APPLICATIONS

The present invention contains subject matter related to Japanese PatentApplication JP 2005-107782 filed in the Japanese Patent Office on Apr.4, 2005, the entire contents of which being incorporated herein byreference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a battery using a separator made ofpolyolefin and the like.

2. Description of the Related Art

In recent years, portable electronic device technology has beensignificantly developed. Accordingly, electronic devices such as mobilephones and notebook computers have started to be recognized as a basictechnology supporting the highly sophisticated information society.Further, research and development for sophisticating these electronicdevices has been actively promoted. In proportion to suchsophistication, the power consumption of these electronic devicescontinues to be increased. On the other hand, these electronic devicesare demanded to be driven for a long time. Therefore, a high energydensity of the secondary battery as a driving power source has beenconsequently demanded.

In view of the occupied volume and the weight of the battery built inthe electronic devices, a higher battery energy density is moredesirable. In these days, since lithium ion secondary batteries have asuperior energy density, the lithium ion secondary battery is built inmost devices.

In general, in the lithium ion secondary battery, lithium cobaltate isused for the cathode, a carbon material is used for the anode, and theoperating voltage is used in the range from 4.2 V to 2.5 V. In anelectric cell, ability to increase the terminal voltage up to 4.2 Vhighly depends on superior chemical stability of the nonaqueouselectrolyte material, the separator and the like.

In traditional lithium ion secondary batteries operating at 4.2 V atmaximum, for the cathode active material such as lithium cobaltate usedfor the cathode, only about 60% of the capacity to the theoreticalcapacity is used. Therefore, in principle, it is possible to utilize theremaining capacity by further increasing the charging voltage. In fact,it is known that a high energy density is realized by setting thevoltage in charging to 4.25 V or more (for example, refer toInternational Publication No. WO03/019713).

SUMMARY OF THE INVENTION

However, in the battery setting the charging voltage over 4.2 V,oxidation atmosphere particularly in the vicinity of the cathode surfaceis intensified. In the result, the separator physically contacting thecathode is oxidized and decomposed. Thereby, there is a disadvantagethat micro short circuit easily occurs particularly under the hightemperature environment, and battery characteristics such as cyclecharacteristics and high temperature storage characteristics arelowered.

In view of the foregoing disadvantage, in the present invention, it isdesirable to provide a battery setting the charging voltage over 4.2 V,which is capable of improving battery characteristics such as cyclecharacteristics and high temperature storage characteristics.

According to an embodiment of the present invention, there is provided abattery in which a cathode and an anode are oppositely arranged with aseparator in between, wherein an open circuit voltage in a full chargestate per a pair of the cathode and the anode is in the range from 4.25V to 6.00 V, and at least part of the cathode side of the separator ismade of at least one from the group consisting of polyvinylidenefluoride, polytetrafluoroethylene, polypropylene, and aramid.

According to the battery of the embodiment of the present invention,since the open circuit voltage in full charge is in the range from 4.25V to 6.00 V, a high energy density can be obtained. Further, since atleast part of the cathode side of the separator is made of at least onefrom the group consisting of polyvinylidene fluoride,polytetrafluoroethylene, polypropylene, and aramid, chemical stabilityof the separator can be improved, and occurrence of micro short circuitcan be inhibited. Therefore, the energy density can be improved, and thebattery characteristics such as cycle characteristics and hightemperature storage characteristics can be improved.

Other and further objects, features and advantages of the invention willappear more fully from the following description.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a cross section showing a structure of a secondary batteryaccording to an embodiment of the present invention;

FIG. 2 is a cross section showing an enlarged part of a spirally woundelectrode body in the secondary battery shown in FIG. 1;

FIG. 3 is an exploded perspective view showing a structure of asecondary battery according to another embodiment of the presentinvention;

FIG. 4 is a cross section taken along line I-I of a spirally woundelectrode body shown in FIG. 3;

FIG. 5 is a characteristics diagram showing float characteristics insecondary batteries fabricated in examples; and

FIG. 6 is a characteristics diagram showing cycle characteristics in asecondary battery fabricated in an example.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

Embodiments of the present invention will be hereinafter described indetail with reference to the drawings.

First Embodiment

FIG. 1 shows a cross sectional structure of a secondary batteryaccording to a first embodiment. The secondary battery is a so-calledlithium ion secondary battery, in which lithium (Li) is used as anelectrode reactant, and the anode capacity is expressed by the capacitycomponent due to insertion and extraction of lithium. The secondarybattery is a so-called cylinder type battery, and has a spirally woundelectrode body 20, in which a pair of a strip-shaped cathode 21 and astrip-shaped anode 22 is wound with a separator 23 in between, inside abattery can 11 in the shape of approximately hollow cylinder. Thebattery can 11 is made of, for example, iron (Fe) plated by nickel (Ni)and one end thereof is closed, and the other end thereof is opened.Inside the battery can 11, a pair of insulating plates 12 and 13 isrespectively arranged perpendicular to the spirally wound peripheryface, so that the spirally wound electrode body 20 is sandwiched betweenthe insulating plates 12 and 13.

At the open end of the battery can 11, a battery cover 14, and a safetyvalve mechanism 15 and a PTC (Positive Temperature Coefficient) device16 provided inside the battery cover 14 are attached by being caulkedthrough a gasket 17. Inside of the battery can 11 is therebyhermetically sealed. The battery cover 14 is made of, for example, amaterial similar to that of the battery can 11. The safety valvemechanism 15 is electrically connected to the battery cover 14 throughthe PTC device 16. When the internal pressure of the battery becomes acertain level or more by internal short circuit, external heating or thelike, a disk plate 15A flips to cut the electrical connection betweenthe battery cover 14 and the spirally wound electrode body 20. Whentemperatures rise, the PTC device 16 limits a current by increasing theresistance value to prevent abnormal heat generation by a large current.The gasket 17 is made of, for example, an insulating material and itssurface is coated with asphalt.

The spirally wound electrode body 20 is wound centering on a center pin24. A cathode lead 25 made of aluminum (Al) or the like is connected tothe cathode 21 of the spirally wound electrode body 20. An anode lead 26made of nickel or the like is connected to the anode 22. The cathodelead 25 is electrically connected to the battery cover 14 by beingwelded to the safety valve mechanism 15. The anode lead 26 is welded andelectrically connected to the battery can 11.

FIG. 2 shows an enlarged part of the spirally wound electrode body 20shown in FIG. 1. The cathode 21 has a structure in which, for example, acathode active material layer 21B is provided on the both faces of acathode current collector 21A having a pair of opposed faces. Though notshown, the cathode active material layer 21B may be provided on only oneface of the cathode current collector 21A. The cathode current collector21A is made of a metal foil such as an aluminum foil. The cathode activematerial layer 21B contains, for example, as a cathode active material,one or more cathode materials capable of inserting and extractinglithium. If necessary, the cathode active material layer 21B contains anelectrical conductor such as graphite and a binder such aspolyvinylidene fluoride.

As a cathode material capable of inserting and extracting lithium, forexample, a lithium-containing compound such as a lithium oxide, alithium phosphorous oxide, a lithium sulfide, and an intercalationcompound containing lithium is appropriate. Two or more thereof may beused by mixing. In order to improve the energy density, alithium-containing compound which contains lithium, transition metalelements, and oxygen (O) is preferable. Specially, a lithium-containingcompound which contains at least one from the group consisting of cobalt(Co), nickel, manganese (Mn), and iron as a transition metal element ismore preferable. Examples of lithium-containing compound include alithium complex oxide having a bedded salt structure shown in Chemicalformula 1, Chemical formula 2, or Chemical formula 3; a lithium complexoxide having a spinel structure shown in Chemical formula 4; a lithiumcomplex phosphate having an olivine structure shown in Chemical formula5 or the like. Specifically, LiNi_(0.50)CO_(0.20)Mn_(0.30)O₂, Li_(a)CoO₂(a≈1), Li_(b)NiO₂ (b≈1), Li_(c1)Ni_(c2)Co_(1-c2)O₂ (c1≈1, 0<c2<1),Li_(d)Mn₂O₄ (d≈1), Li_(e)FePO₄ (e≈1) or the like can be cited.

(Chemical Formula 1)Li_(f)Mn_((1-g-h))Ni_(g)M1_(h)O_((2-j))F_(k)

In the formula, M1 represents at least one from the group consisting ofcobalt, magnesium (Mg), aluminum, boron (B), titanium (Ti), vanadium(V), chromium (Cr), iron, copper (Cu), zinc (Zn), zirconium (Zr),molybdenum (Mo), tin (Sn), calcium (Ca), strontium (Sr), and tungsten(W). f, g, h, j, and k are values in the range of 0.8≦f≦1.2, 0≦g≦0.5,0≦h≦0.5, g+h≦1, −0.1≦j≦0.2, and 0≦k≦0.1. The composition of lithiumvaries according to charge and discharge states. A value of f representsthe value in a full discharge state.

Chemical Formula 2Li_(m)Ni_((1-n))M2_(n)O_((2-p))F_(q)

In the formula, M2 represents at least one from the group consisting ofcobalt, manganese, magnesium, aluminum, boron, titanium, vanadium,chromium, iron, copper, zinc, molybdenum, tin, calcium, strontium, andtungsten. m, n, p, and q are values in the range of 0.8≦m≦1.2,0.005≦n≦0.5, −0.1≦p≦0.2, and 0≦q≦0.1. The composition of lithium variesaccording to charge and discharge states. A value of m represents thevalue in a full discharge state.

Chemical Formula 3Li_(r)Co_((1-s))M3_(s)O_((2-t))F_(u)

In the formula, M3 represents at least one from the group consisting ofnickel, manganese, magnesium, aluminum, boron, titanium, vanadium,chromium, iron, copper, zinc, molybdenum, tin, calcium, strontium, andtungsten. r, s, t, and u are values in the range of 0.8≦r≦1.2, 0≦s<0.5,−0.1≦t≦0.2, and 0≦u≦0.1. The composition of lithium varies according tocharge and discharge states. A value of r represents the value in a fulldischarge state.

(Chemical Formula 4)Li_(v)Mn_(2-w)M4_(w)O_(x)F_(y)

In the formula, M4 represents at least one from the group consisting ofcobalt, nickel, magnesium, aluminum, boron, titanium, vanadium,chromium, iron, copper, zinc, molybdenum, tin, calcium, strontium, andtungsten. v, w, x, and y are values in the range of 0.9≦v≦1.1, 0≦w≦0.6,3.7≦x≦4.1, and 0≦y≦0.1. The composition of lithium varies according tocharge and discharge states. A value of v represents the value in a fulldischarge state.

Chemical Formula 5Li_(z)M5PO₄

In the formula, M5 represents at least one from the group consisting ofcobalt, manganese, iron, nickel, magnesium, aluminum, boron, titanium,vanadium, niobium, copper, zinc, molybdenum, calcium, strontium,tungsten, and zirconium. z is a value in the range of 0.9≦z≦1.1. Thecomposition of lithium varies according to charge and discharge states.A value of z represents the value in a full discharge state.

As a cathode material capable of inserting and extracting lithium, inaddition to the foregoing, an inorganic compound not containing lithiumsuch as MnO₂, V₂O₅, V₆O₁₃, NiS, and MoS can be cited.

The anode 22 has a structure in which an anode active material layer 22Bis provided on the both faces of an anode current collector 22A having apair of opposed faces. Though not shown, the anode active material layer22B may be provided only on one face of the anode current collector 22A.The anode current collector 22A is made of, for example, a metal foilsuch as a copper foil

The anode active material layer 22B contains, as an anode activematerial, one or more anode materials capable of inserting andextracting lithium. If necessary, the anode active material layer 22Bcontains a binder similar to of the cathode active material layer 21B.

In the secondary battery, the electrochemical equivalent of the anodematerial capable of inserting and extracting lithium is larger than theelectrochemical equivalent of the cathode 21. In the middle of charge,lithium metal is not precipitated on the anode 22.

Further, in the secondary battery, the open circuit voltage when fullycharged (that is, battery voltage) is designed to fall within the rangefrom 4.25 V to 6.00 V. Therefore, the lithium extraction amount per unitweight is larger than in the battery in which the open circuit voltagewhen fully charged is 4.20 V even though the same cathode activematerial is used. Accordingly, the amounts of the cathode activematerial and the anode active material are adjusted. Thereby, a higherenergy density can be obtained.

As an anode material capable of inserting and extracting lithium, forexample, a carbon material such as non-graphitizable carbon,graphitizable carbon, graphite, pyrolytic carbons, cokes, glassycarbons, an organic high molecular weight compound fired body, carbonfiber, and activated carbon can be cited. Of the foregoing, cokesinclude pitch cokes, needle cokes, petroleum cokes and the like. Theorganic high molecular weight compound fired body is obtained by firingand carbonizing a high molecular weight material such as a phenol resinand a furan resin at an appropriate temperature, and some of them arecategorized as non-graphitizable carbon or graphitizable carbon. As ahigh molecular weight material, polyacetylene, polypyrrole or the likecan be cited. These carbon materials are preferable, since a change inthe crystal structure occurred in charge and discharge is very small, ahigh charge and discharge capacity can be obtained, and favorable cyclecharacteristics can be obtained. In particular, graphite is preferable,since the electrochemical equivalent is large, and a high energy densitycan be obtained. Further, non-graphitizable carbon is preferable sincesuperior characteristics can be obtained. Furthermore, a material with alow charge and discharge potential, specifically a material with thecharge and discharge potential close to of lithium metal is preferable,since a high energy density of the battery can be easily realized.

As an anode material capable of inserting and extracting lithium, amaterial which is capable of inserting and extracting lithium, andcontains at least one of metal elements and metalloid elements as anelement can be also cited. When such a material is used, a high energydensity can be obtained. In particular, such a material is morepreferably used together with a carbon material, since a high energydensity can be obtained, and superior cycle characteristics can beobtained. Such an anode material may be a simple substance, an alloy, ora compound of a metal element or a metalloid element, or may have one ormore phases thereof at least in part. In the present invention, alloysinclude an alloy containing one or more metal elements and one or moremetalloid elements, in addition to an alloy including two or more metalelements. Further, an alloy may contain nonmetallic elements. Thetexture thereof includes a solid solution, a eutectic crystal (eutecticmixture), an intermetallic compound, and a tecture in which two or morethereof coexist.

As a metal element or a metalloid element composing the anode material,for example, magnesium, boron, aluminum, gallium (Ga), indium (In),silicon (Si), germanium (Ge), tin, lead (Pb), bismuth (Bi), cadmium(Cd), silver (Ag), zinc, hafnium (Hf), zirconium, yttrium (Y), palladium(Pd), or platinum (Pt) can be cited. They may be crystalline oramorphous.

Specially, as the anode material, a material containing a metal elementor a metalloid element of Group 4B in the short period periodic table asan element is preferable. A material containing at least one of siliconand tin as an element is particularly preferable. Silicon and tin have ahigh ability to insert and extract lithium, and can obtain a high energydensity.

As an alloy of tin, for example, an alloy containing at least one fromthe group consisting of silicon, nickel, copper, iron, cobalt,manganese, zinc, indium, silver, titanium (Ti), germanium, bismuth,antimony (Sb), and chromium as a second element other than tin can becited. As an alloy of silicon, for example, an alloy containing at leastone from the group consisting of tin, nickel, copper, iron, cobalt,manganese, zinc, indium, silver, titanium, germanium, bismuth, antimony,and chromium as a second element other than silicon can be cited.

As a compound of tin or a compound of silicon, for example, a compoundcontaining oxygen (O) or carbon (C) can be cited. In addition to tin orsilicon, the compound may contain the foregoing second element.

As an anode material capable of inserting and extracting lithium, othermetal compound or a high molecular weight material can be further cited.As other metal compound, an oxide such as MnO₂, V₂O₅, and V₆O₁₃; asulfide such as NiS and MoS; or a lithium nitride such as LiN₃ can becited. As a high molecular weight material, polyacetylene, polyaniline,polypyrrole or the like can be cited.

The separator 23 has a base material layer 23A and a surface layer 23Bprovided on the face of the base material layer 23A, which is opposed tothe cathode 21, or the both faces of the base material layer 23A. Thesurface layer 23B may be provided on the entire surface or on part ofthe surface of the base material layer 23A. In FIG. 2, the surface layer23B is provided only on the face of the base material layer 23A, whichis opposed to the cathode 21.

The base material layer 23A is made of, for example, a porous film madeof a synthetic resin such as polypropylene and polyethylene. The basematerial layer 23A may have a structure in which two or more porousfilms as the foregoing porous films are layered. Specially, thepolyolefin porous film is preferable since the polyolefin porous filmhas a superior short circuit prevention effect and is capable ofimproving safety of the battery by shut down effect. In particular, as amaterial of the base material layer 23A, polyethylene is preferable,since polyethylene obtains shutdown effects in the range from 100 deg C.to 160 deg C. and has superior chemical stability. Further,polypropylene is also preferable. In addition, as long as a resin haschemical stability, such a resin may be used by being copolymerized withpolyethylene or polypropylene, or by being blended with polyethylene orpolypropylene.

The surface layer 23B contains at least one from the group consisting ofpolyvinylidene fluoride, polytetrafluoroethylene, polypropylene, andaramid. Thereby, chemical stability is improved, and occurrence of microshort circuit is inhibited. When the surface layer 23B is formed frompolypropylene, the base material layer 23A may be formed frompolypropylene, and is structured as a monolayer.

The thickness of the surface layer 23B on the side opposed to thecathode 21 is preferably in the range from 0.1 μm to 10 μm. When thethickness is small, the effect of inhibiting occurrence of micro shortcircuit is small. Meanwhile, when the thickness is large, the ionconductivity is lowered, and the volume capacity is lowered.

The thickness of the separator 23 is preferably in the range from 5 μmto 25 μm. When the thickness is small, short circuit may occur.Meanwhile, when the thickness is large, the ion conductivity is lowered,and the volume capacity is lowered. The air permeability of theseparator 23 is preferably in the range from 200 sec/100 cm³ to 600sec/100 cm³ as a value converting to the thickness of 20 μm. When theair permeability is low, short circuit may occur. Meanwhile, when theair permeability is high, the ion conductivity is lowered. Furthermore,the porosity of the separator 23 is preferably in the range from 30% to60%. When the porosity is low, the ion conductivity is lowered.Meanwhile, when the porosity is high, short circuit may occur. Inaddition, the piercing strength of the separator 23 is preferably in therange from 0.020 N/cm² to 0.061 N/cm² as a value converting to thethickness of 20 μm. When the piercing strength is low, short circuit mayoccur. Meanwhile, when the piercing strength is high, the ionconductivity is lowered.

An electrolytic solution as a liquid electrolyte is impregnated in theseparator 23. The electrolytic solution contains, for example, a solventand an electrolyte salt dissolved in the solvent.

As a solvent, for example, a cyclic ester carbonate such as ethylenecarbonate and propylene carbonate can be used. One of ethylene carbonateand propylene carbonate is preferably used. In particular, the mixtureof the both is more preferably used. Thereby, cycle characteristics canbe improved.

As a solvent, further, a chain ester carbonate such as diethylcarbonate, dimethyl carbonate, ethyl methyl carbonate, and methyl propylcarbonate is preferably mixed with the foregoing cyclic ester carbonate.Thereby, high ion conductivity can be obtained.

As a solvent, furthermore, 2,4-difluoro anisole or vinylene carbonate ispreferably contained. 2,4-difluoro anisole can improve the dischargecapacity, and vinylene carbonate can improve the cycle characteristics.Therefore, a mixture of 2,4-difluoro anisole and vinylene carbonate ispreferably used, since the discharge capacity and the cyclecharacteristics can be improved.

In addition, as other solvent, butylene carbonate, γ-butyrolactone,γ-valerolactone, 1,2-dimethoxyethane, tetrahydrofuran, 2-methyltetrahydrofuran, 1,3-dioxolan, 4-methyl-1,3-dioxolan, methyl acetate,methyl propionate, acetonitrile, glutaronitrile, adiponitrile, methoxyacetonitrile, 3-methoxy propylonitrile, N,N-dimethylformamide,N-methylpyrolidinone, N-methyl oxazolidinone, N,N-dimethylimidazolidinone, nitromethane, nitroethane, sulfolane, dimethylsulfoxide, and trimethyl phosphate can be cited.

In some cases, a compound obtained by substituting at least part ofhydrogen of the foregoing solvent with fluorine is preferable, sincesuch a compound may improve reversibility of electrode reactiondepending on the electrode type to be combined.

As an electrolyte salt, for example, a lithium salt can be cited. Onelithium salt may be used singly, or two or more lithium salts may beused by mixing. As a lithium salt, LiPF₆, LiBF₄, LiAsF₆, LiClO₄,LiB(C₆H₅)₄, LiCH₃SO₃, LiCF₃SO₃, LiN(SO₂CF₃)₂, LiC(SO₂CF₃)₃, LiAlCl₄,LiSiF₆, LiCl, lithium difluoro[oxalato-O,O′] borate, lithium bis oxalateborate, LiBr or the like can be cited. Specially, LiPF₆ is preferablesince high ion conductivity can be obtained, and the cyclecharacteristics can be improved.

The secondary battery can be manufactured, for example, as follows.

First, for example, a cathode active material, an electrical conductor,and a binder are mixed to prepare a cathode mixture, which is dispersedin a solvent such as N-methyl-2-pyrrolidone to obtain a paste cathodemixture slurry. Next, the cathode current collector 21A is coated withthe cathode mixture slurry, the solvent is dried, and the resultant iscompression-molded by a rolling press machine or the like to form thecathode active material layer 21B and thereby forming the cathode 21.

Further, for example, an anode active material and a binder are mixed toprepare an anode mixture, which is dispersed in a solvent such asN-methyl-2-pyrrolidone to obtain paste anode mixture slurry. Next, theanode current collector 22A is coated with the anode mixture slurry, thesolvent is dried, and the resultant is compression-molded by a rollingpress machine or the like to form the anode active material layer 22Band thereby forming the anode 22.

Subsequently, the cathode lead 25 is attached to the cathode currentcollector 21A by welding or the like, and the anode lead 26 is attachedto the anode current collector 22A by welding or the like. After that,the cathode 21 and the anode 22 are wound with the separator 23 inbetween. The end of the cathode lead 25 is welded to the safety valvemechanism 15, and the end of the anode lead 26 is welded to the batterycan 11. The wound cathode 21 and the wound anode 22 are sandwichedbetween the pair of insulating plates 12 and 13, and contained insidethe battery can 11. After the cathode 21 and the anode 22 are containedinside the battery can 11, an electrolytic solution is injected into thebattery can 11 and impregnated in the separator 23. After that, at theopen end of the battery can 11, the battery cover 14, the safety valvemechanism 15, and the PTC device 16 are fixed by being caulked throughthe gasket 17. The secondary battery shown in FIG. 1 is therebycompleted.

In the secondary battery, when charged, lithium ions are extracted fromthe cathode active material layer 21B and inserted in the anode materialcapable of inserting and extracting lithium contained in the anodeactive material layer 22B through the electrolytic solution. Next, whendischarged, the lithium ions inserted in the anode material capable ofinserting and extracting lithium in the anode active material layer 22Bis extracted, and inserted in the cathode active material layer 21Bthrough the electrolytic solution. Here, since the separator 23 has theforegoing structure, the chemical stability is improved. Even when theopen circuit voltage when fully charged is increased, occurrence ofmicro short circuit is inhibited, and the battery characteristics areimproved.

As above, in this embodiment, since the open circuit voltage when fullycharged is in the range from 4.25 V to 6.00 V. Therefore, a high energydensity can be obtained. Further, the layer made of at least one fromthe group consisting of polyvinylidene fluoride,polytetrafluoroethylene, polypropylene, and aramid is provided on atleast the side of the separator, which is opposed to the cathode 21.Therefore, chemical stability of the separator 23 can be improved, andoccurrence of micro short circuit can be inhibited. Consequently, theenergy density can be improved, and the battery characteristics such ascycle characteristics and high temperature storage characteristics canbe improved.

Second Embodiment

A secondary battery according to a second embodiment of the presentinvention is a so-called lithium metal secondary battery, in which theanode capacity is expressed by the capacity component due toprecipitation and dissolution of lithium as an electrode reactant.

The secondary battery has a structure and effects similar to of thesecondary battery according to the first embodiment, except that theanode active material layer 22B has a different structure. Therefore,descriptions will be given by using the same symbols for thecorresponding components with reference to FIG. 1 and FIG. 2.Descriptions of the same components will be omitted.

The anode active material layer 22B is formed from lithium metal as ananode active material, and can obtain a high energy density. The anodeactive material layer 22B may already exist when the battery isassembled. Otherwise, it is possible that the anode active materiallayer 22B does not exist when assembling the battery, and is made oflithium metal precipitated when the battery is charged. Otherwise, it ispossible that the anode active material layer 22B is utilized as acurrent collector and the anode current collector 22A is omitted.

The secondary battery can be manufactured in the same manner as thesecondary battery according to the first embodiment, except that theanode 22 is made of only the anode current collector 22A, made of onlylithium metal, or made by forming the anode active material layer 22B bybonding lithium metal to the anode current collector 22A.

In the secondary battery, when charged, for example, lithium ions areextracted from the cathode 21 and precipitated as lithium metal on thesurface of the anode current collector 22A through the electrolyticsolution. In the result, the anode active material layer 22B is formedas shown in FIG. 2. When discharged, for example, lithium metal iseluted as lithium ions from the anode active material layer 22B, andinserted in the cathode 21 through the electrolytic solution. Here,since the separator 23 has the foregoing structure, the chemicalstability is improved. Even when the open circuit voltage in full chargeis increased, occurrence of micro short circuit is inhibited, and thebattery characteristics are improved.

Third Embodiment

A secondary battery according to a third embodiment of the presentinvention is a secondary battery, in which the anode capacity includesthe capacity component due to insertion and extraction of lithium as anelectrode reactant and the capacity component due to precipitation anddissolution of lithium, and is expressed by the sum thereof.

The secondary battery has a structure and effects similar to of thesecondary battery of the first or the second embodiment, except that thestructure of the anode active material layer is different, and can besimilarly manufactured. Therefore, here, descriptions will be given byusing the same symbols with reference to FIG. 1 and FIG. 2. Detaileddescriptions for the same components will be omitted.

In the anode active material layer 22B, for example, by setting thecharging capacity of the anode material capable of inserting andextracting lithium to the value smaller than the charging capacity ofthe cathode 21, lithium metal begins to be precipitated on the anode 22when the open circuit voltage (that is, battery voltage) is lower thanthe overcharge voltage in the charging process. Therefore, in thesecondary battery, both the anode material capable of inserting andextracting lithium and lithium metal function as an anode activematerial, and the anode material capable of inserting and extractinglithium is a base material when the lithium metal is precipitated.

The overcharge voltage means the open circuit voltage when the batteryovercharged. For example, the overcharge voltage means a higher voltagethan the open circuit voltage of the battery, which is “fully charged,”described in and defined by “Guideline for Safety Assessment of lithiumsecondary batteries” (SBA G1101), which is one of the guidelinesspecified by Japan Storage Battery Industries Incorporated (Batteryassociation of Japan). In other words, the overcharge voltage means ahigher voltage than the open circuit voltage after charge by usingcharging method used in obtaining nominal capacities of each battery, astandard charging method, or a recommended charging method.

The secondary battery is similar to traditional lithium ion secondarybatteries in view of using the anode material capable of inserting andextracting lithium for the anode 22. Further, the secondary battery issimilar to traditional lithium metal secondary batteries in view thatlithium metal is precipitated on the anode 22. However, in the secondarybattery, lithium metal is precipitated on the anode material capable ofinserting and extracting lithium. Thereby, a high energy density can beobtained, and cycle characteristics and rapid charge characteristics canbe improved.

In the secondary battery, when charged, lithium ions are extracted fromthe cathode 21, and firstly inserted in the anode material capable ofinserting and extracting lithium contained in the anode 22 through theelectrolytic solution. When further charged, in a state that the opencircuit voltage is lower than the overcharge voltage, lithium metalbegins to be precipitated on the surface of the anode material capableof inserting and extracting lithium. After that, until charge isfinished, lithium metal continues to be precipitated on the anode 22.Next, when discharged, first, lithium metal precipitated on the anode 22is eluted as ions, which are inserted in the cathode 21 through theelectrolytic solution. When further discharged, lithium ions inserted inthe anode material capable of inserting and extracting lithium in theanode 22 are extracted, and inserted in the cathode 21 through theelectrolytic solution. Here, since the separator 23 has the foregoingstructure, the chemical stability is improved. Even when the opencircuit voltage in full charge is increased, occurrence of micro shortcircuit is inhibited, and the battery characteristics are improved.

Fourth Embodiment

FIG. 3 shows a structure of a secondary battery according to a fourthembodiment of the present invention. In the secondary battery, aspirally wound electrode body 30 on which a cathode lead 31 and an anodelead 32 are attached is contained inside a film package member 40.Therefore, the size, the weight, and the thickness thereof can bereduced.

The cathode lead 31 and the anode lead 32 are respectively directed frominside to outside of the package member 40 in the same direction, forexample. The cathode lead 31 and the anode lead 32 are respectively madeof, for example, a metal material such as aluminum, copper, nickel, andstainless, and are in the shape of thin plate or mesh.

The package member 40 is made of a rectangular aluminum laminated film,in which, for example, a nylon film, an aluminum foil, and apolyethylene film are bonded together in this order. The package member40 is, for example, arranged so that the polyethylene film side and thespirally wound electrode body 30 are opposed, and the respective outeredges are contacted to each other by fusion bonding or an adhesive.Adhesive films 41 to protect from outside air intrusion are insertedbetween the package member 40 and the cathode lead 31, the anode lead32. The adhesive film 41 is made of a material having contactcharacteristics to the cathode lead 31 and the anode lead 32, forexample, is made of a polyolefin resin such as polyethylene,polypropylene, modified polyethylene, and modified polypropylene.

The exterior member 40 may be made of a laminated film having otherstructure, a high molecular weight film such as polypropylene, or ametal film, instead of the foregoing aluminum laminated film.

FIG. 4 shows a cross sectional structure taken along line I-I of thespirally wound electrode body 30 shown in FIG. 3. In the spirally woundelectrode body 30, a pair of cathode 33 and anode 34 are layered with aseparator 35 and an electrolyte layer 36 in between and wound. Theoutermost periphery thereof is protected by a protective tape 37.

The cathode 33 has a structure in which a cathode active material layer33B is provided on one face or both faces of a cathode current collector33A. The anode 34 has a structure, in which an anode active materiallayer 34B is provided on one face or both faces of an anode currentcollector 34A. Arrangement is made so that the anode active materiallayer 34B side is opposed to the cathode active material layer 33B. Thestructures of the cathode current collector 33A, the cathode activematerial layer 33B, the anode current collector 34A, the anode activematerial layer 34B, and the separator 35 are similar to of the cathodecurrent collector 21A, the cathode active material layer 21B, the anodecurrent collector 22A, the anode active material layer 22B, and theseparator 23 respectively described in the first to the thirdembodiments.

The electrolyte layer 36 is so-called gelatinous, containing anelectrolytic solution and a high molecular weight compound to become aholding body, which holds the electrolytic solution. The gelatinouselectrolyte layer 36 is preferable, since high ion conductivity can beobtained and liquid leakage of the battery can be prevented. Thecomposition of the electrolytic solution (that is, a solvent, anelectrolyte salt and the like) is similar to of the secondary batteriesaccording to the first to the third embodiments. As a high molecularweight compound, for example, polyacrylonitrile, polyvinylidenefluoride, a copolymer of polyvinylidene fluoride andhexafluoropropylene, polytetrafluoroethylene, polyhexafluoropropylene,polyethylene oxide, polypropylene oxide, polyphosphazene, polysiloxane,polyvinyl acetate, polyvinyl alcohol, polymethylmethacrylate,polyacrylic acid, polymethacrylic acid, styrene-butadiene rubber,nitrile-butadiene rubber, polystyrene, or polycarbonate can be cited. Inparticular, in view of chemical stability, polyacrylonitrile,polyvinylidene fluoride, polyhexafluoropropylene, or polyethylene oxideis preferable.

The secondary battery can be manufactured, for example, as follows.

First, the cathode 33 and the anode 34 are respectively coated with aprecursor solution containing a solvent, an electrolyte salt, a highmolecular weight compound, and a mixed solvent. The mixed solvent isvolatilized to form the electrolyte layer 36. After that, the cathodelead 31 is welded to the end of the cathode current collector 33A, andthe anode lead 32 is welded to the end of the anode current collector34A. Next, the cathode 33 and the anode 34 formed with the electrolytelayer 36 are layered with the separator 35 in between to obtain alamination. After that, the lamination is wound in the longitudinaldirection, the protective tape 37 is adhered to the outermost peripherythereof to form the spirally wound electrode body 30. Lastly, forexample, the spirally wound electrode body 30 is sandwiched between thepackage members 40, and outer edges of the exterior members 40 arecontacted by thermal fusion bonding or the like to enclose the spirallywound electrode body 30. Then, the adhesive films 41 are insertedbetween the cathode lead 31, the anode lead 32 and the exterior member40. Thereby, the secondary battery shown in FIG. 3 and FIG. 4 iscompleted.

Otherwise, the secondary battery may be fabricated as follows. First,the cathode 33 and the anode 34 are formed as described above, and thecathode lead 31 and the anode lead 32 are attached on the cathode 33 andthe anode 34. After that, the cathode 33 and the anode 34 are layeredwith the separator 35 in between and wound. The protective tape 37 isadhered to the outermost periphery thereof, and a spirally wound body asa precursor of the spirally wound electrode body 30 is formed. Next, thespirally wound body is sandwiched between the exterior members 40, theperipheral edges except for one side are thermally fusion-bonded toobtain a pouched state, and the spirally wound body is contained insidethe exterior member 40. Subsequently, an electrolytic compositioncontaining a solvent, an electrolyte salt, a monomer as a raw materialfor the high molecular weight compound, a polymerization initiator, andif necessary other material such as a polymerization inhibitor isprepared, which is injected into the package member 40.

After the electrolytic composition is injected, the opening of thepackage member 40 is thermally fusion-bonded and hermetically sealed inthe vacuum atmosphere. Next, the resultant is heated to polymerize themonomer to obtain a high molecular weight compound. Thereby, thegelatinous electrolyte layer 36 is formed, and the secondary batteryshown in FIG. 3 is assembled.

The secondary battery provides action and effects similar to of thesecondary batteries according to the first to the third embodiments.

EXAMPLES

Further, specific examples of the present invention will be described indetail.

Examples 1-1 to 1-4

Batteries, in which the capacity of the anode 22 was expressed by thecapacity component due to insertion and extraction of lithium, that is,so-called lithium ion secondary batteries were fabricated. Then, thebattery shown in FIG. 1 was fabricated.

First, a cathode active material was formed. As an aqueous solution,commercially available nickel nitrate, cobalt nitrate, and manganesenitrate were mixed so that the mol ratios of Ni, Co, Mn became 0.50,0.20, and 0.30, respectively. After that, while the mixture wassufficiently agitated, ammonia water was dropped into the mixed solutionto obtain a complex hydroxide. The complex hydroxide and lithiumhydroxide were mixed, the mixture was fired for 10 hours at 900 deg C.by using an electric furnace, and pulverized to obtain lithium complexoxide powder as a cathode active material. When the obtained lithiumcomplex oxide powder was analyzed by Atomic Absorption Spectrometry(ASS), the composition of LiNi_(0.50)Co_(0.20)Mn_(0.30)O₂ was verified.Further, when the particle diameter was measured by laser diffractionmethod, the average particle diameter was 13 μm. Further, when X-raydiffraction measurement was conducted, it was confirmed that themeasurement result was similar to the pattern of LiNiO₂ listed in No.09-0063 of the ICDD (International Center for Diffraction Data) card,and a layered sodium chloride structure similar to of LiNiO₂ was formed.Furthermore, when the obtained lithium complex oxide powder was observedby Scanning Electron Microscope (SEM), spherical particles, in whichprimary particles being from 0.1 μm to 5 μm in size were aggregated,were observed.

The obtained LiNi_(0.50)Co_(0.20)Mn_(0.30)O₂ powder, graphite as anelectrical conductor, polyvinylidene fluoride as a binder were mixed ata weight ratio of LiNi_(0.50)Co_(0.20)Mn_(0.30)O₂powder:graphite:polyvinylidene fluoride=86:10:4 to prepare a cathodemixture. Subsequently, the cathode mixture was dispersed inN-methyl-2-pyrrolidone as a solvent to obtain cathode mixture slurry.The both faces of the cathode current collector 21A made of astrip-shaped aluminum foil being 20 μm thick were uniformly coated withthe cathode mixture slurry, which was dried and compress-molded by arolling press machine to form the cathode active material layer 21B andthereby forming the cathode 21. The thickness of the cathode 21 was 150μm. After that, the cathode lead 25 made of aluminum was attached to oneend of the cathode current collector 21A.

Further, spheroidal graphite powder being 30 μm in average particlediameter as an anode active material and polyvinylidene fluoride as abinder were mixed at a weight ratio of spheroidal graphitepowder:polyvinylidene fluoride=90:10 to prepare an anode mixture.Subsequently, the anode mixture was dispersed in N-methyl-2-pyrrolidoneas a solvent to obtain anode mixture slurry. The both faces of the anodecurrent collector 22A made of a strip-shaped copper foil being 15 μmthick were uniformly coated with the anode mixture slurry, which wasprovided with hot press molding to form the anode active material layer22B and thereby forming the anode 22. The thickness of the anode 22 was160 μm. After that, the anode lead 26 made of nickel was attached to oneend of the anode current collector 22A. The electrochemical equivalentratio between the cathode 21 and the anode 22 was designed so that thecapacity of the anode 22 was expressed by the capacity component due toinsertion and extraction of lithium.

After the cathode 21 and the anode 22 were respectively formed, theseparator 23 made of a microporous film was prepared. Then, the anode22, the separator 23, the cathode 21, and the separator 23 were layeredin this order, and the resultant lamination was spirally wound manytimes. Thereby, the jelly roll type spirally wound electrode body 20 wasformed. As shown in Table 1, in Example 1-1, the separator 23 in whichthe both faces of the base material were coated with polyvinylidenefluoride so that each thickness of the coat became 2 μm was used. InExample 1-2, the separator 23 in which the base material face on theside opposed to the cathode 21 was coated with polytetrafluoroethyleneso that the thickness of the coat became 7 μm was used. In Example 1-3,the separator 23 in which the both faces of the base material werecoated with polypropylene so that each thickness of the coat became 2 μmwas used. In Example 1-4, the separator 23 in which the base materialface on the side opposed to the cathode 21 was coated with aramid sothat the thickness of the coat became 3 μm was used. For the basematerial, polyethylene being 16 μm thick was used. TABLE 1 Surface layerBase material Cathode side Anode side Example 1-1 PolyethylenePolyvinylidene fluoride Polyvinylidene fluoride Example 1-2Polytetrafluoroethylene — Example 1-3 Polypropylene PolypropyleneExample 1-4 Aramid — Comparative Polyethylene — — example 1-1

After the spirally wound electrode body 20 was formed, the spirallywound electrode body 20 was sandwiched between the pair of insulatingplates 12 and 13. The anode lead 26 was welded to the battery can 11,the cathode lead 25 was welded to the safety valve mechanism 15, and thespirally wound electrode body 20 was contained inside the battery can 11made of nickel-plated iron. After that, 4.0 g of an electrolyticsolution was injected into the battery can 11 by depressurizationmethod.

For the electrolytic solution, an electrolytic solution obtained bydissolving LiPF₆ as an electrolyte salt in a mixed solvent of ethylenecarbonate, dimethyl carbonate, and vinylene carbonate at a weight ratioof ethylene carbonate:dimethyl carbonate:vinylene carbonate=35:60:1 sothat LiPF₆ became 1.5 mol/kg was used.

After the electrolytic solution was injected into the battery can 11, bycaulking the battery can 11 with the battery cover 14 through the gasket17 with the surface coated with asphalt, cylinder type secondarybatteries being 14 mm in diameter and 65 mm in height were obtained forExamples 1-1 to 1-4.

As Comparative example 1-1 relative to Examples 1-1 to 1-4, a secondarybattery was fabricated in the same manner as in Examples 1-1 to 1-4,except that polyethylene being 16 μm thick was used as the separator 23.

For the obtained secondary batteries of Examples 1-1 to 1-4 andComparative example 1-1, high temperature storage characteristics andcycle characteristics were examined.

For high temperature storage characteristics, after constant currentcharge was performed by a constant current of 1000 mA until the batteryvoltage reached 4.4 V in the constant temperature bath set at 60 deg C.,constant voltage charge was performed at 4.4 V. Then, fluctuations ofthe charging current values, that is, float characteristics wereobtained. The results are shown in FIG. 5.

For cycle characteristics, after constant current charge was performedat a constant current of 1000 mA until the battery voltage reached 4.40V, constant voltage charge was performed for 1 hour at a constantvoltage of 4.40 V. Subsequently, constant current discharge wasperformed at a constant current of 2000 mA until the battery voltagereached 3 V. Such charge and discharge were repeated. The dischargecapacity retention ratio at a given cycle to the discharge capacity atthe first cycle was obtained as (discharge capacity at a givencycle/discharge capacity at the first cycle)×100 (%). The results ofExample 1-3 and Comparative example 1-1 are shown in FIG. 6.

As evidenced by FIG. 5, in Examples 1-1 to 1-4 using the separator 23,in which the base material was coated with polyvinylidene fluoride,polypropylene, polytetrafluoroethylene, or aramid, when time lapsed, thecharging current rise was not shown. Meanwhile, in Comparative example1-1 using the separator, in which the base material was not coated withpolyvinylidene fluoride, polypropylene, polytetrafluoroethylene, oraramid, it was confirmed that when about 70 hours lapsed, chargingcurrent rise was shown, and micro short circuit occurred.

Further, as evidenced by FIG. 6, according to Example 1-3 using theseparator 23, in which the base material was coated with polypropylene,decrease in the discharge capacity retention ratio corresponding torepetition of cycles was smaller than in Comparative example 1-1 usingthe separator, in which the base material was not coated withpolypropylene.

That is, it was found that in the battery, in which the open circuitvoltage in full charge was in the range from 4.25 V to 6.00 V, when atleast part of the cathode side of the separator 23 was made of at leastone from the group consisting of polyvinylidene fluoride,polytetrafluoroethylene, polypropylene, and aramid, batterycharacteristics such as cycle characteristics and high temperaturestorage characteristics could be improved.

The present invention has been described with reference to theembodiments and the examples. However, the present invention is notlimited to the foregoing embodiments and the foregoing examples, andvarious modifications may be made. For example, in the foregoingembodiments and the foregoing examples, descriptions have been given ofthe case using lithium as an electrode reactant. However, the presentinvention can be applied to the case using other Group 1A element suchas sodium (Na) and potassium (K), a Group 2A element such as magnesiumand calcium (Ca), other light metal such as aluminum, or an alloy oflithium or the foregoing as well, and similar effects can be therebyobtained. Then, for the anode active material, the anode material asdescribed in the foregoing embodiments can be similarly used.

Further, in the foregoing embodiments and the foregoing examples,descriptions have been given of the secondary battery having thespirally wound structure. However, the present invention can besimilarly applied to a secondary battery having a structure in which acathode and an anode are folded or a secondary battery having astructure in which a cathode and an anode are layered. In addition, thepresent invention can be applied to a secondary battery such as aso-called coin type battery, a button type battery, and a square typebattery.

It should be understood by those skilled in the art that variousmodifications, combinations, sub-combinations and alternations may occurdepending on design requirements and other factors insofar as they arewithin the scope of the appended claims or the equivalents thereof.

1. A battery in which a cathode and an anode are oppositely arrangedwith a separator in between, wherein an open circuit voltage in a fullcharge state per a pair of the cathode and the anode is in the rangefrom 4.25 V to 6.00 V, and at least part of the cathode side of theseparator is made of at least one from the group consisting ofpolyvinylidene fluoride, polytetrafluoroethylene, polypropylene, andaramid.
 2. The battery according to claim 1, wherein the separator has:a base material layer made of a polyolefin porous film; and a surfacelayer which is provided on the cathode side of the base material layer,and is made of at least one from the group consisting of polyvinylidenefluoride, polytetrafluoroethylene, polypropylene, and aramid.
 3. Thebattery according to claim 2, wherein the base material layer containsat least one of polyethylene and polypropylene.
 4. The battery accordingto claim 1, wherein the anode contains a carbon material.
 5. The batteryaccording to claim 1, wherein the anode contains at least one from thegroup consisting of graphite, graphitizable carbon, andnon-graphitizable carbon.